Integra SL specifications may vary due to local regulatory requirements.


Please contact Direx's Office in your local area for further information regarding the modification and limitation of the system.



Integra SL Regulatory Approval:
CE - Europe


Vertex X-ray Unit Regulatory Approval:
CE - Europe
FDA - USA


FDA Regulatory Approval

INTEGRA SPECIFICATIONS
Integrated Unit
Principle of OperationElectromagnetic generator
Transducer : Elco-2Hollow/Non Cylindrical type
Therapeutical Focal AreaUser Selectable 6,9,12,15,18mm
Penetration Depth 160mm
Shock Wave Triggering 1Hz - 2Hz and ECG Synchronized
X-Ray GeneratorHigh Frequency 40Khz
X-ray Tube Rotating Anode,
Focus 0.3 and 0.6 mm
X-Ray kV Range 40-110 KV
X-Ray mA Range4mA - 10 mA
Image Intensifier9"
CCD cameraDigital, 1K x 1K x 10 bits
Gantry Assembly 3 axis (X,Y,Z) digitally controlled
Assembly Range 100mm X,Y,Z
Patient Positioning on TableLeft/Right Stones in
same position
Table Dimensions 78 cm x 200 cm
Alignment and Calibration Not required


Control Unit
PC ProcessorPentium 4/2.8 Ghz
Monitor20" High Resolution
Flat Panel TFT Brightness,
Contrast, Gamma, Zoom Unlimited
Sequential Treatment Pictures Mathematical Filers :
Median, Edge, Enhancement, Equalization, Clean…
Positive / Negative Image
Rotate Distance Measurements
Patient Record Database5000 Patient records
Connectivity DICOM 3 (optional)


GENERAL
Line Requirements115/230V, 50-60 Hz 1 Phase
Electrical SafetyIEC 601.1